US2230624A - Extraction of protein from peanuts - Google Patents

Extraction of protein from peanuts Download PDF

Info

Publication number
US2230624A
US2230624A US254741A US25474139A US2230624A US 2230624 A US2230624 A US 2230624A US 254741 A US254741 A US 254741A US 25474139 A US25474139 A US 25474139A US 2230624 A US2230624 A US 2230624A
Authority
US
United States
Prior art keywords
protein
solution
peanuts
alkaline
extraction
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US254741A
Other languages
English (en)
Inventor
Mclean Andrew
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Application granted granted Critical
Publication of US2230624A publication Critical patent/US2230624A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23JPROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
    • A23J1/00Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites
    • A23J1/14Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from leguminous or other vegetable seeds; from press-cake or oil-bearing seeds
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F4/00Monocomponent artificial filaments or the like of proteins; Manufacture thereof

Definitions

  • This invention relates to the extraction of proteins from peanuts; and it comprises a method of extracting the globulins in colorless form from residues left in regaining oil from peanuts wherein the residues are extracted with an alkaline aqueous solution at a pH not exceeding 8.5 at anytime and being 8 to 8.5'in the final stages of the extraction, and recovering the globulins from the solution so formed by acidification,
  • the globulins (arachin and conarachin) contained in peanuts (Arachis) have been found ,--*to be an advantageous material for the production of artificial fibers, much like wool in their properties and susceptible of being dyed, spun, woven, etc., in much the same manner as wool. In these methods a light-colored material of reasonable purity is desirable. A light color is particularly necessary.
  • protein from peanuts is dissolved or dispersed in urea solutions. The urea acts as a denaturant, changing the physical form of the globulin molecule of the protein into one better adapted for mak ing filaments.
  • the protein gives a thin dispersion which can be clarified to free it of mechanical impurities and gradually thickens on ageing into a form suitable for extrusion.
  • the aged solution is extruded in the ordinary Ways used in making filaments; extrusion being into an aqueous bath adapted to remove the urea. There may or may not be some acid in this bath and the filaments may afterwards he treated in 5 various ways not here important.
  • the urea acts as a solvent or peptizing agent. The solvent action may be accelerated by small amounts of othermaterials not here important.
  • the object achieved in the present invention is the production of a high yield of light colored
  • protein from peanut residues left after extracting oil either residues from blanched or from unblanched nuts.
  • the protein removed in the present invention is particularly applicable for fiber-making operations.
  • Suitable alkaline materials for use according to my invention are mild or caustic alkalis, such as sodium hydroxide or carbonate, or ammonia, l5 and strongly alkaline salts such as sodium sulfide; alkaline substances strong enough to enable maintenance of the specified pH during the extraction.
  • a mixture of indicators such as one of th so-called universal indicators, may be used to follow the change in alkalinity of the solution, or I may use an indicator such as Phenol Red 45 or Cresol Red to show the final stage of the extraction, in conjunction with a more acid indicator such as litmus or Bromthymol Blue (yellow to blue, 6.0-7.6) which gives warning when the acidic material in the nut meal is approach- 50 ing exhaustion.
  • the mixture When the mixture has been maintained at the desired alkalinity for a time suflicient for substantially complete extraction of the protein soluble at that alkalinity, the mixture may be setof protein forms.
  • the insoluble matter may be stirred up with water and again centrifuged, and the washings added to the main solution; which may then be clarified in e. g. a super-centrifuge of the high-speed type.
  • the soluble protein may then be reprecipitated from the solution by a suitable change in the alkalinity; for instance by neutralizing the alkali with sulphur dioxide, or by allowing acid-forming fermentation to occur in the solution.
  • the progress of the neutralization may be followed by means of a suitable external indicator; for instance, Methyl Orange (red to yellow, 3.0-4.4) or Bromphenol Blue (yellow to blue 3.0-4.7).
  • a suitable external indicator for instance, Methyl Orange (red to yellow, 3.0-4.4) or Bromphenol Blue (yellow to blue 3.0-4.7).
  • Example 1 200 parts of extracted peanut meal from unblanched nuts are stirred vigorously with 3500 parts water at 20 C. for 5 to minutes. 330 parts of a 1.2 per cent solution of sodium sul phide are run in over a period of 14 minutes. During the addition hydrogen sulphide is evolved, and the mixture does not appreciably affect the color of red litmus. The bath is not alkaline to litmus. Further addition of the sodium sulphide solution, however, causes a marked rise in the pH value, and the rate of addition of alkali is therefore reduced. At the end of 30 minutes 170 parts of sodium sulphide solution have been added, and the pH value of the solution is found to be approximately 8.0 to 8.5.
  • Example 2 200 parts extracted peanut meal from unblanched nuts are stirred vigorously with 3500 parts water at 20 C. as in Example 1.
  • 150 parts of a 1.2 per cent solution of sodium hydroxide in water are added over a period of 20 minutes while the mixture is kept stirred.
  • the pH value reaches a value of about 8.0-8.5 at the end of the operation. Stirring is continued for one hour.
  • After clarification the solution has a pH value of 8.3, and the solution is almost entirely devoid of undesirable color.
  • Sulphur dioxide is passed through the solution until the pH value is 4.5, also in the iso-electric region; and the white precipitate of protein is worked up as in Example 1.
  • the dry product amounts to 84 parts by weight and is white in color, yielding almost colorless solution in concentrated aqueous urea, which on standing becomes unusually viscous before it gelates. This is an advantageous property.
  • the solution may be spun into filaments or excellent color and quality.
  • Example 1 instead of the sodium sulphide used in Example 1, I could have used sodium hydroxide, sodium polysulphide, sodium carbonate, sodium cyanide, or the hydroxides or salts of the alkalis and alkaline earths. The point is maintenance of the specified pH range during the extraction rather than the use of any particular alkaline substance. Any salt chosen should of coursebe one without ill effect on the protein.
  • This invention is a valuable advance in the art as it enables the protein to be extracted from peanuts by a simple process which omits the expensive blanching step.
  • the resulting protein has better spinning qualities than those produced by old methods and will form spinning solutions from which filaments of excellent appearance and physical properties may be obtained by a wet spinning process.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Peptides Or Proteins (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
US254741A 1938-02-16 1939-02-04 Extraction of protein from peanuts Expired - Lifetime US2230624A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4882/38A GB513896A (en) 1938-02-16 1938-02-16 Improvements in or relating to the extraction of protein from ground nuts

Publications (1)

Publication Number Publication Date
US2230624A true US2230624A (en) 1941-02-04

Family

ID=9785608

Family Applications (1)

Application Number Title Priority Date Filing Date
US254741A Expired - Lifetime US2230624A (en) 1938-02-16 1939-02-04 Extraction of protein from peanuts

Country Status (5)

Country Link
US (1) US2230624A (en(2012))
DE (1) DE898946C (en(2012))
FR (1) FR850388A (en(2012))
GB (1) GB513896A (en(2012))
NL (1) NL52770C (en(2012))

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2417576A (en) * 1943-04-12 1947-03-18 Ici Ltd Manufacture of viscous protein solutions for the production of artificial filaments
US2431993A (en) * 1947-12-02 Alkali-treating vegetable protein
US2603630A (en) * 1948-12-31 1952-07-15 Robert S Aries Method for extracting proteins from yeast
US2628022A (en) * 1953-02-10 Method fob recovering protein from
US2684960A (en) * 1954-07-27 Method of isolating protein from

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE417950A (en(2012)) * 1935-10-22

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2431993A (en) * 1947-12-02 Alkali-treating vegetable protein
US2628022A (en) * 1953-02-10 Method fob recovering protein from
US2684960A (en) * 1954-07-27 Method of isolating protein from
US2417576A (en) * 1943-04-12 1947-03-18 Ici Ltd Manufacture of viscous protein solutions for the production of artificial filaments
US2603630A (en) * 1948-12-31 1952-07-15 Robert S Aries Method for extracting proteins from yeast

Also Published As

Publication number Publication date
GB513896A (en) 1939-10-25
FR850388A (fr) 1939-12-15
NL52770C (en(2012))
DE898946C (de) 1953-12-07

Similar Documents

Publication Publication Date Title
US2230624A (en) Extraction of protein from peanuts
US2459754A (en) Purification of phenol sulfides and preparation of metallic salts thereof
US1990367A (en) Method of refining rosin
US2406650A (en) Method for the extraction of casein from seeds
US2127641A (en) Process for obtaining high grade sulphuric acid esters
DE827254C (de) Verfahren zur Gewinnung von Gummi aus Gummimagermilch
US1777757A (en) Indophenol intermediate and blue sulphur dye derived therefrom
US1452481A (en) Manufacture of 1.4 naphthol sulphonic acid
US2055746A (en) Sulphur dye preparations
US2152693A (en) Production of sulphur dyes
USRE16040E (en) And elmer g
US2156071A (en) Sulphur dyes from hydroxydiarylamines
US1949243A (en) Production of alpha naphthol
US2578661A (en) Cyclic reuse of cyclohexylamine in rosin acids separation
US1716492A (en) Production of a basic copper sulphate
GB537740A (en) Improvements in or relating to the production of solutions for the manufacture of artificial fibres, and artificial fibres derived therefrom
US1412949A (en) Manufacture of soluble condensation products
US2202594A (en) Pigments for use in manufacture of artificial silk
US2320980A (en) Manufacture of neutral blanc fixe
US2154616A (en) Grease-setting agent
US1996822A (en) Separation of 1, 8-naphthylamine-sulphonic acid
DE495366C (de) Verfahren zur Herstellung von Benzanthronderivaten
US2441671A (en) Process for preparing sulfonamides
US1957547A (en) Improved dibenzanthrone and process for its manufacture
US1776904A (en) Sulphurized dyestuffs and method of making the same